Luteolin supplementation during porcine oocyte maturation improves the developmental competence of parthenogenetic activation and cloned embryos

Luteolin (Lut), a polyphenolic compound that belongs to the flavone subclass of flavonoids, possesses anti-inflammatory, cytoprotective, and antioxidant activities. However, little is known regarding its role in mammalian oocyte maturation. This study examined the effect of Lut supplementation during in vitro maturation (IVM) on oocyte maturation and subsequent developmental competence after somatic cell nuclear transfer (SCNT) in pigs. Lut supplementation significantly increased the proportions of complete cumulus cell expansion and metaphase II (MII) oocytes, compared with control oocytes. After parthenogenetic activation or SCNT, the developmental competence of Lut-supplemented MII oocytes was significantly enhanced, as indicated by higher rates of cleavage, blastocyst formation, expanded or hatching blastocysts, and cell survival, as well as increased cell numbers. Lut-supplemented MII oocytes exhibited significantly lower levels of reactive oxygen species and higher levels of glutathione than control MII oocytes. Lut supplementation also activated lipid metabolism, assessed according to the levels of lipid droplets, fatty acids, and ATP. The active mitochondria content and mitochondrial membrane potential were significantly increased, whereas cytochrome c and cleaved caspase-3 levels were significantly decreased, by Lut supplementation. These results suggest that Lut supplementation during IVM improves porcine oocyte maturation through the reduction of oxidative stress and mitochondria-mediated apoptosis.


INTRODUCTION
Because of their physiological and anatomical similarities to humans, transgenic pigs generated by somatic cell nuclear transfer (SCNT) have been used in many areas of biomedical research, including bioreactors, human disease models, and xenotransplantation (Gil et al., 2010;Meurens et al., 2012). In parallel, numerous attempts have been made to increase the developmental competence of SCNT embryos, resulting in the increased production of cloned piglets; however, efficiency remains low compared with in vivo embryo production (Grupen, 2014;Whitworth & Prather, 2010). One reason for this low efficiency is the inadequate in vitro maturation (IVM) environment of oocytes (Herrick, 2019). Oocyte maturation is a complex process that involves both nuclear and cytoplasmic maturation. The low developmental competence of IVM oocytes leads to failed embryonic development, mainly because of improper cytoplasmic maturation despite complete nuclear maturation (Gilchrist & Thompson, 2007). Successful cytoplasmic maturation depends on the IVM environment and thus on the medium composition and culture conditions (Maedomari et al., 2007;Marchal et al., 2001). Optimal IVM conditions are therefore the most important determinant of successful oocyte maturation and a prerequisite for the increased efficiency of transgenic pig production.
Reactive oxygen species (ROS) are commonly generated from byproducts of intracellular energy metabolism, and specifically from the byproducts of mitochondrial respiration in aerobic organisms. Although ROS at moderate levels are essential intracellular signaling molecules involved in normal biological processes, their excessive accumulation (from disrupted redox homeostasis) leads to oxidative stress and thus potentially to cytoskeletal abnormalities, lipid peroxidation, adenosine 5′-triphosphate (ATP) depletion, mitochondrial dysfunction, and apoptosis (Park et al., 2021;Wang et al., 2021). In the in vivo environment, the female reproductive tract (ovary, oviduct, and uterus) protects against ROS accumulation through its antioxidant defense system (Agarwal et al., 2012). However, during IVM, an imbalance between ROS generation and antioxidant activity can induce oxidative stress (Tarin et al., 1996). Compared with other species, the oocytes of pigs are much more sensitive to physiological stress, such as the stress caused by excess light, abnormal oxygen tension, and sudden changes in pH, because of their high cellular lipid and fatty acid contents (Sturmey et al., 2009). Stress-induced excessive ROS generation leads to embryonic arrest or lower embryo viability (Byrne et al., 1999). Attempts to reduce oxidative damage by dietary supplementation with numerous ROS scavengers, such as resveratrol, melatonin, and ascorbic acid, have failed to yield IVM conditions compare to the in vivo environment (Kere et al., 2013;Lee et al., 2018). An understanding of oxidative stress defense mechanisms and the application of more effective antioxidants would protect oocytes against oxidative stress while improving IVM.
Flavonoids are polyphenol secondary metabolites widely distributed in fruits, vegetables, and herbs (de Rijke et al., 2006). Many animals, including humans, consume significant amounts of flavonoids, which are present in a wide variety of edible plants (Mutha, Tatiya & Surana, 2021). The flavonoid luteolin (3,4,5,Lut) belongs to the flavone group and is abundant in many vegetables and fruits, especially broccoli, carrots, and rosemary. Lut has been reported to have many biological functions including anti-inflammatory, antibacterial, anti-cancer, antioxidant, and cytoprotective activities (Gupta et al., 2018;Huang, Kim & Cho, 2023). Most previous studies of Lut have focused on therapeutic agents due to its potent anti-cancer and anti-inflammatory activities. Deqiu et al. (2011) reported that Lut can ameliorate insulin resistance-related endothelial dysfunction. Chen et al. (2014) reported that Lut effectively protects mice from lipopolysaccharide-induced lethality by suppressing heat shock protein 90 activity. Kim et al. (2018) reported that Lut suppresses airway inflammation by regulating immune response. In addition, the antioxidant activity of Lut reflects its ability to reduce free radical formation and thus oxidative stress in human umbilical vein endothelial cells and neuroblastoma cells (Chen et al., 2020;Zhang et al., 2013). Although the physiological and biological roles of Lut are well-documented in many cell types, the effect of Lut during meiotic maturation in pigs has not been investigated.
This study examined the effects of Lut supplementation on oocyte maturation and the subsequent developmental competence of SCNT embryos in pigs. Lut was added to the maturation medium; its effects on nuclear maturation, cumulus cell expansion, and subsequent embryonic development after parthenogenetic activation (PA) and SCNT were determined based on intracellular ROS and glutathione (GSH) levels, lipid metabolism, mitochondrial function, and activation of the apoptosis pathway in Lut-treated porcine oocytes.

Ethics statement
This study was conducted in strict accordance with the recommendations of the Korea Research Institute of Bioscience and Biotechnology (KRIBB) Institutional Animal Care and Use Committee (approval no. KRIBB-AEC-21107).

Chemicals
All chemicals and reagents used in the present study were acquired from Sigma-Aldrich Chemical Company (St. Louis, MO, USA), unless otherwise indicated.

Oocyte collection and in vitro maturation
Oocyte collection and in vitro maturation were performed as described previously (Park et al., 2021). Porcine ovaries were retrieved from a local slaughterhouse and transported to the laboratory in 0.9% NaCl supplemented with potassium penicillin (75 µg/mL) and streptomycin sulfate (50 µg/mL) at 38.5 C within 2 h. Cumulus-oocyte complexes (COCs) were recovered from antral follicles (about 3-6 mm in diameter) using an 18-gauge needle fixed to a 10-mL disposable syringe. The COCs were washed three times in 0.9% NaCl supplemented with 0.1% bovine serum albumin (BSA), after which~50 COCs were matured in 500 µL IVM medium in a four-well multi-dish (Nunc, Roskilde, Denmark) for without hormones for another 22 h.

Luteolin (Lut) treatment
The concentration of Lut was chosen according to a previous study (Park et al., 2021). Lut was dissolved in dimethyl sulfoxide, then diluted in IVM medium to a final concentration of 5 µM Lut (along with 0.1% dimethyl sulfoxide).

Assessment of cumulus cell expansion and the nuclear maturation of oocytes
Cumulus cell expansion and nuclear maturation were assessed as described previously, with modifications (Jeong et al., 2020a). After 44 h of IVM, the degree of cumulus cell expansion in porcine COCs was observed by morphological examination under a microscope (Nikon Corp., Tokyo, Japan) and classified as follows: grade 1: no expansion; grade 2: poor expansion, with spherical and compacted cumulus cells around the oocyte; grade 3: partial expansion, with the expansion of cumulus cell layers except the corona radiata; grade 4: full expansion of all cumulus cell layers. For assessment of nuclear maturation, cumulus cells after 44 h of IVM were removed by gentle pipetting with 0.1% hyaluronidase in Dulbecco's phosphate-buffered saline (DPBS; Gibco, Grand Island, NY, USA) supplemented with 4 mg/mL BSA. The denuded oocytes were examined under a microscope (Nikon Corp., Tokyo, Japan) and classified as degenerate, immature (without first polar body extrusion), or MII stage.

Somatic cell nuclear transfer
SCNT was performed as described previously, with modifications (Jeong et al., 2020b(Jeong et al., , 2021(Jeong et al., , 2017. MII oocytes in DPBS supplemented with 4 mg/mL BSA, 75 µg/mL penicillin G, 50 µg/mL streptomycin sulfate, and 7.5 µg/mL cytochalasin B were cut using a sharp pipette and then the first polar body and cytoplasm-containing chromosomes were removed using the squeezing method under an inverted microscope (DMI 3000B; Leica Microsystems, Wetzlar, Germany) equipped with a micromanipulator (NT-88-V3; Nikon Narishige, Tokyo, Japan). We used KRIBB small miniature pig kidney cells established in a previous study as donor cells (Song et al., 2018). Donor cell injection and fusion were conducted using the Sendai virus (SV)-mediated method. Briefly, the freeze-dried inactivated SV envelope was dissolved in 260 mL of suspending buffer and diluted 1:4 (v/v) with cell fusion buffer, in accordance with the manufacturer's instructions (Cosmo Bio, Osaka, Japan). Donor cells were immersed in the inactivated SV solution for 1 min, then introduced into the perivitelline space of cytoplasts. After 2 h, oocyte-cell couplets that had completely fused, as confirmed using an inverted microscope, were selected and activated for 4 h in activation medium containing 1 µM oxamflatin at 38.5 C in 5% CO 2 in air. The activated embryos were transferred to IVC medium supplemented with 1 mM oxamflatin, cultured for 20 h, washed in fresh IVC medium and then cultured in IVC medium at 38.5 C in 5% CO 2 in air. Cleavage and blastocyst rates were determined at 48 and 144 h, respectively.

Indirect immunofluorescence assay
Indirect immunofluorescence assay was performed as described previously (Jeong et al., 2021). Oocytes or blastocysts were fixed in 4% paraformaldehyde overnight at 4 C and washed three times for 10 min each in DPBS supplemented with 1 mg/mL PVA (DPBS-PVA). The fixed oocytes/blastocysts were permeabilized by incubation for 1 h at RT in PBS containing 0.5% Triton X-100. After three washes in DPBS-PVA, the oocytes/blastocysts were stored overnight at 4 C in DPBS-PVA supplemented with 1 mg/mL BSA (DPBS-PVA-BSA). For CDX2 staining, blastocysts were blocked with 10% normal goat serum for an additional 45 min, then incubated at 4 C overnight with cytochrome c (Abcam, Cambridge, UK), cleaved caspase 3 (Cell Signaling Technology, Danvers, MA, USA) or mouse monoclonal anti-CDX2 (Biogenex Laboratories Inc., San Ramon, CA, USA) as the primary antibody. After three washes in DPBS-PVA-BSA, the oocytes/blastocysts were incubated for 1 h at room temperature (RT) with conjugated secondary antibody, either Alexa-Fluor-488-labeled goat anti-mouse or anti-rabbit IgG (1:200 in DPBS-PVA-BSA), washed three times for 10 min each in DPBS-PVA-BSA, stained for DNA using 2 µg/mL DAPI, and observed using a fluorescence microscope (Olympus, Tokyo, Japan).
Terminal deoxynucleotidyl transferase-mediated dUTP-digoxygenin nick end-labeling (TUNEL) assay TUNEL assay was conducted using an in situ cell death detection kit (Roche, Basel, Switzerland), as described previously (Jeong et al., 2021). Fixed Blastocysts were washed three times for 10 min each in DPBS-PVA and were incubated in DPBS containing 0.5% Triton X-100 for 1h at RT. After three washes for 10 min each in DPBS-PVA, they were incubated in DPBS containing 10 mg/mL BSA for 1 h at RT. Blastocysts were incubated with TUNEL reaction medium for 1 h at 38.5 C, washed three for 10 min each in DPBS-PVA, and mounted on clean glass slides with DAPI. Whole-mount blastocysts were observed under a fluorescence microscope (Olympus, Tokyo, Japan) by using detection for DAPI labeled (total cell numbers) or TUNEL positive (apoptotic cell numbers) nuclei. Five to 10 blastocysts per treatment group were used in the TUNEL assay in each independent experiment.

Measurement of intracellular ROS and GSH levels
The oocytes were washed three times with DPBS-PVA and incubated in DPBS-PVA containing 5 mM CM-H2DCFDA (Invtrogene, Carlsbad, CA, USA) for 30 min or 10 mM CMF2HC (Invitrogen, Waltham, MA, USA) for 10 min. After incubation, the oocytes were washed three times with DPBS-PVA. Fluorescence images were captured with a fluorescence microscope (DMi8; Leica Microsystems) equipped with an ultraviolet filter (460 nm for ROS or 370 nm for GSH). Fluorescence intensity was analyzed using ImageJ software (version 1.47; National Institutes of Health, Bethesda, MD, USA).
Analysis of ATP, lipid droplet, and fatty acid contents ATP, lipid droplet, and fatty acid analysis were performed as described previously (Joo et al., 2023). The oocytes were washed three times in DPBS-PVA and fixed in 4% paraformaldehyde overnight at 4 C. For ATP staining, the fixed oocytes were washed three times in DPBS-PVA and incubated for 1 h at RT in the dark in DPBS containing 500 nM BODIPY FL ATP (BODIPY-ATP; A12410; Molecular Probes, Eugene, OR, USA). Subsequently, the oocytes were washed three times with DPBS-PVA, mounted on clean glass slides, and stained with DAPI. For lipid droplet and fatty acid staining, the fixed oocytes were washed three times in DPBS-PVA and incubated for 1 h at RT in the dark in DPBS containing 10 mg/mL BODIPY 493/503 (BODIPY-LD; D3922; Molecular Probes, Eugene, OR, USA) or 6 mM BODIPY 558/568 C12 (BODIPY-FA; D3835; Molecular Probes, Eugene, OR, USA). After three washes in DPBS-PVA, the oocytes were mounted on glass slides and imaged using a fluorescence microscope (DMi8; Leica Microsystems, Wetzlar, Germany). Fluorescence intensity was analyzed using ImageJ software after data normalization via subtraction of background intensity from each oocyte size.

Analysis of mitochondria content and mitochondrial membrane potential
MitoTracker and JC-1 staining were performed as described previously (Jeong et al., 2019). The oocytes were incubated for 1 h in DPBS-PVA containing MitoTracker Red CMXRos (Invitrogen, Waltham, MA, USA) or JC-1 (1:100) (Cayman Chemical, Ann Arbor, MI, USA), washed three times for 10 min each in DPBS-PVA, and fixed for 2 h at RT in 4% paraformaldehyde. After three more 10 min washes in DPBS-PVA, the oocytes were either immediately observed under a fluorescence microscope (DMi8; Leica Microsystems, Wetzlar, Germany) for JC-1 staining or mounted on glass slides in Vectashield containing DAPI (Vector Laboratories, Newark, CA, USA) and then observed under a fluorescence microscope (DMi8; Leica Microsystems, Wetzlar, Germany) for MitoTracker staining. Fluorescence intensity was analyzed using ImageJ software after data normalization via subtraction of background intensity from each oocyte size.

Statistical analyses
All experiments were repeated at least three times. The results are expressed as means ± standard errors of the mean. Data were analyzed by analysis of variance, followed by Student's t-test, using SigmaStat software (SPSS Inc., Chicago, IL, USA). P-values < 0.05 were considered indicative of statistical significance.

Luteolin enhances the mitochondrial functions of porcine oocytes
As sites of oxidative phosphorylation, mitochondria are essential to cellular energy production during oocyte maturation and subsequent embryonic development. Accordingly, the effects of Lut on the developmental competence of porcine oocytes during IVM were examined by measuring both the mitochondrial content and mitochondrial membrane potential. Compared with the control group, the mitochondrial content of Lut-supplemented oocytes was higher (Con, 53.8 ± 2.8 vs. Lut, 66.6 ± 3.9) (Figs. 5A and 5B) and the J-aggregate (high membrane potential)/J-monomer (low membrane potential) ratio was significantly increased (Con, 1.50 ± 0.01 vs. Lut, 1.64 ± 0.01) (Figs. 5C and 5D). Luteolin protects mitochondrial-mediated apoptosis of porcine oocytes The effects of Lut on the apoptosis pathway were assessed by measuring the levels of cytochrome c and cleaved caspase-3 in porcine MII oocytes. Cytochrome c levels were lower in Lut-supplemented oocytes than in control MII oocytes (Con, 85.9 ± 3.1 vs. Lut, 76.7 ± 2.1) (Figs. 6A and 6B); cleaved caspase-3 levels were also lower in Lut-supplemented oocytes (Con, 10.3 ± 0.4 vs. Lut, 8.8 ± 0.4) (Figs. 6C and 6D).

DISCUSSION
The production of transgenic pigs by SCNT has attracted interest from biomedical researchers; however, the production efficiency resulting from this approach is suboptimal because of factors related to oocyte quality and culture conditions. Poor IVM conditions are mainly the result of the oxidative stress induced by the overproduction of ROS, which disrupts normal cell structures and processes, including cell membranes, RNA transcription, DNA/protein synthesis, and lipid metabolism, leading to decreased oocyte quality (Guerin, El Mouatassim & Menezo, 2001). Previous studies showed that antioxidant supplementation during IVM allows the successful cytoplasmic maturation of porcine oocytes and enhances the developmental capacity of SCNT embryos by reducing ROS levels (Kere et al., 2013;Qi et al., 2020;Taweechaipaisankul et al., 2016). Lut is a powerful antioxidant with excellent radical-scavenging and cytoprotective abilities (Heim, Tagliaferro & Bobilya, 2002). Luteolin has a double bond between C2 and C3 that provides hydrogen/electrons, and can stabilize the radical group by blocking the Fenton reaction using the oxo group of C4 that binds to transition metal ions such as iron and copper (Gendrisch et al., 2021). These structural features of Lut prevent oxidative damage by inhibiting pro-oxidant enzymes and inducing antioxidant enzymes. A previous study reported that Lut upregulates the transcription of ROS scavenging enzymes by activating the SIRT and FOXO families in human monocytes (Kim, Lee & Yun, 2017). Moreover, the antioxidant abilities of Lut are synergistically reinforced by its interactions with other antioxidants, including vitamins and cellular redox systems (Wolfle, Haarhaus & Schempp, 2013). The results of this study demonstrated that Lut supplementation during IVM improves porcine oocyte maturation and subsequent embryonic development after PA and SCNT. These effects can be at least partly attributed to the benefits conferred by the reduction of oxidative stress on lipid metabolism and mitochondrial function. The cumulus cells surrounding the oocyte provide nutrients, hormones, and an optimal microenvironment for oocyte growth and maturation (Assidi, Dieleman & Sirard, 2010). A previous study showed that the removal of cumulus cells before IVM decreases the oocyte maturation rate and subsequent embryonic development after fertilization, indicating that cumulus cells are crucial for oocyte maturation and quality (Wongsrikeao et al., 2005). Cumulus cell expansion has been used as a morphological indicator of oocyte quality, based on the direct correlation of the optimal expansion of cumulus cells with proper oocyte maturation and the acquisition of developmental competence (Brown et al., 2017). Cumulus cells also play an important role in protecting oocytes from environmental stress, including oxidative stress (Tatemoto, Sakurai & Muto, 2000). However, excessive oxidative stress in cumulus cells induced cellular apoptosis and reduced CX43 levels (gap junction related factors), resulting in reduced oocyte quality (Qian et al., 2022). Moreover, oxidative stress caused by hydrogen peroxide exposure reduced not only expression of cumulus cell expansion-and maternal factor-related genes but also blastocyst formation and total cell number; interestingly, isorhamnetin treatment, another flavonoid compound, rescued by these defects (Oh et al., 2023). In this study, Lut supplementation prevents oxidative stress in porcine COCs by reducing ROS levels and increasing GSH levels. Moreover, Lut supplementation during IVM significantly increased the rate of COCs with fully expanded cumulus cells and MII oocytes, which then improved porcine IVM efficiency by reducing oxidative stress.
Oocyte quality is gradually acquired during ovarian follicular development, which includes oocyte growth and maturation (Eppig et al., 1994). Both preimplantation embryonic development and pregnancy maintenance to full term can be traced to oocyte quality. Although many transgenic pigs obtained by SCNT have been produced from IVM-derived oocytes, only a small percentage of those oocytes develop to the blastocyst stage, suggesting that current IVM systems do not adequately support the acquisition of oocyte developmental competence (Trounson, Anderiesz & Jones, 2001). Improving oocyte quality would thus increase the rate of successful embryonic development after SCNT. This study showed that, in PA and SCNT embryos, Lut supplementation during IVM significantly increases the cleavage rate, blastocyst formation, proportions of expanded or hatching blastocysts, cell number, and cellular survival rate; these results demonstrate the beneficial effects of Lut on the developmental competence of PA and SCNT embryos through enhancement of oocyte quality.
Lipid droplets are crucial organelles that store oocyte intracellular lipids to regulate cellular metabolism and energy homeostasis. During oocyte maturation, oocytes synthesize lipid droplets using fatty acids, liquid-liquid phase separation and lipid accumulation in the membrane of the endoplasmic reticulum. Simultaneously, fatty acids are cleaved from triglycerides by lipase activation and transported into the mitochondria, where they undergo β-oxidation for the ATP production that is necessary to support successful oocyte growth and maturation (Ferguson & Leese, 2006). Abnormal lipid metabolism, including elevated levels of saturated fatty acids, impairs oocyte maturation and quality, thus interrupting subsequent embryonic development (Bradley & Swann, 2019). Immature porcine oocytes are particularly sensitive to the damage caused by oxidative stress because their lipid contents are much higher than the contents in other mammalian species, including cows, mice, and sheep, suggesting an important role for lipid metabolism in porcine oocyte maturation (McEvoy et al., 2000;Somfai et al., 2011). The significantly higher contents of lipid droplets, fatty acids, and ATP in Lut-supplemented oocytes, compared with control MII oocytes, suggest that the improved IVM efficiency achieved by Lut supplementation is mediated by enhancement of lipid metabolism. However, further detailed experiments are needed to provide direct evidence of the effects of Lut supplementation on lipid metabolism during porcine oocyte maturation.
Mitochondria are cytoplasmic organelles that regulate ATP synthesis, ROS generation, calcium signaling, fatty acid oxidation, apoptosis, and other cellular metabolic processes (McBride, Neuspiel & Wasiak, 2006). They also support important aspects of mammalian reproduction, including oocyte maturation, fertilization, and embryonic development (Van Blerkom, 2011). However, oxidative stress by excessive ROS accumulation triggers a decrease in cellular mitochondrial content through the suppression of mitochondrial biogenesis involving mtDNA replication, membrane formation, and mitochondrial division (Bouchez & Devin, 2019;Nisoli et al., 2004). Oxidative stress also disrupts the mitochondrial membrane potential, which reduces the oxidative phosphorylation reaction and ATP synthesis (Aiken, Cindrova-Davies & Johnson, 2008). Numerous studies have reported that antioxidant supplementation during IVM is commonly able to overcome mitochondria injury by reducing ROS levels (Chen et al., 2022;Li et al., 2022;Liu et al., 2023). A previous study reported that Lut increased PGC-1a and nitric oxide levels, which would correct cellular impairment and may reduce mitochondrial ROS production, suggesting that Lut may promote mitochondrial biogenesis (Suh, Chon & Choi, 2016). Our results showed that Lut-supplemented oocytes not only reduced ROS levels but also increased mitochondrial number and membrane potential compared to the control, indicating that Lut supplementation increased mitochondrial number and function due to its antioxidant activity. In addition, oxidative stress disrupts the mitochondrial membrane potential, resulting in the release of cytochrome c from the mitochondria into the cytoplasm (Liu et al., 1996). Cytochrome c is a member of the mitochondria-dependent apoptotic pathway; its activation triggers the caspase cascade, including caspase-9 and caspase-3, to induce apoptosis (Sun et al., 2018). A previous study reported that Lut suppressed lysophosphatidylcholine-induced apoptosis by blocking calcium/ mitochondria/caspase-dependent pathway in human umbilical vein endothelial cells (Song et al., 2010). In this study, Lut supplementation significantly reduced the levels of cytochrome c and cleaved caspase-3 compared to the control, thereby preventing apoptosis. Taken together, these results indicate that Lut supplementation during IVM improves oocyte quality by enhancing mitochondrial function through the reduction of intracellular ROS levels.

CONCLUSIONS
Our results demonstrate that Lut supplementation during IVM improves porcine oocyte quality and subsequent embryonic development after PA and SCNT. The positive effects of Lut can be attributed to the reduction of oxidative stress and enhancements of both lipid metabolism and mitochondrial function. These findings strongly suggest that Lut supplementation can improve the production of high-quality porcine oocytes, thus be used to improve the production of transgenic pigs for biomedical research.